Actively Recruiting
SAPHIR2 : Simplification of PHysical Activity Assessment by Rapid Interrogation
Led by University Hospital, Angers · Updated on 2025-12-29
118
Participants Needed
3
Research Sites
75 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A multicentric, non-interventional study using a clinical questionnaire (SAPHIR) and activity monitor (Activ-PAL) to estimate the level of physical activity in the general population. This study compares the level of physical activity reported by the SAPHIR questionnaire with the activity recorded by the activity monitor during the same period, in order to determine if the SAPHIR score is able to represent the measured physical activity, in a simple and easily calculable manner. Hypothesis: The aim of this work is to propose a new questionnaire that is simple to complete by the patient,quick to analyse and directly calculable by the doctor and adapted to the general population, whether during the initial evaluation or the follow-up. Indeed, these scores are rarely used outside the context of the prescription of physical activity in specialized centers. Moreover, a tool suited to the constraints of community medicine seems necessary, given the growth of the prescription of physical activity in primary care. The idea behind this new questionnaire is to obtain a score ranging from 0 to 100 that can be calculated through simple mental arithmetic, which is not the case for most existing questionnaires, in particular the IPAQ.
CONDITIONS
Official Title
SAPHIR2 : Simplification of PHysical Activity Assessment by Rapid Interrogation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients referred for a consultation at one of the participating centers
- Patients over 18 years old with no upper age limit
You will not qualify if you...
- Patients with a contraindication to walking
- Professional athletes or patients participating in endurance sports competitions
- Patients refusing to participate in the study
- Patients unable to understand the objectives or instructions of the study
- Patients with Activ-PAL recordings of less than 3 days
AI-Screening
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Trial Site Locations
Total: 3 locations
1
CHU d'Angers
Angers, France, 49933
Actively Recruiting
2
CH de Cholet
Cholet, France, 49325
Not Yet Recruiting
3
CH du Mans
Le Mans, France, 72037
Not Yet Recruiting
Research Team
S
Simon LECOQ, MD
CONTACT
A
Anthéa LOIEZ
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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